combined the 454 sequencing technology with paired-end mapping to detect structural variation in the human genome, for an October 2007 study published in Science. “The technology allowed us to ...

This course will give an introduction to the theory and practice of analyzing high-throughput RNA sequencing through lectures and hands-on exercises. The basic topics covered will include: 1) the ...

A new study shows that long-read sequencing has the potential to improve the rate of diagnosis while reducing the time to diagnosis from years to days -- in a single test and at a much lower cost.

This course will give an introduction to the theory and practice of analyzing high-throughput RNA sequencing through lectures and hands-on exercises. The basic topics covered will include: 1) the ...

Explore how nanopore sequencing is revolutionizing microbial genomics! Join Richard Chalvignac as he covers NO-MISS workflows, avian flu surveillance, 16S/ITS sequencing, and more. Live Q&A included.

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

Cancer is a disease of the genome, according to Dr. Elli Papaemmanuil, computational oncologist at MSK. By looking at the ...

Dr. Aaron Wenger tells us about SPRQ chemistry, highlighting its unique benefits and role in expanding our understanding of ...

Metagenomic datasets could help map out microbial diversity hotspots. Published January 17, 2025 in Science Advances, ...

environmental science and so on. It also earned its inventor, Kary B. Mullis, the Nobel Prize in Chemistry in 1993. Before PCR, the process of DNA sequencing was very lengthy and quite expensive.